ENST00000270357.10:c.1627G>T
MANE Select
|
ENSP00000270357.4:p.Glu543Ter
|
|
ENST00000270357.8:c.934G>T
|
ENSP00000270357.3:p.Glu312Ter
|
|
ENST00000437406.1:c.193G>T
|
ENSP00000403319.1:p.Glu65Ter
|
|
ENST00000451363.5:c.268G>T
|
ENSP00000414661.1:p.Glu90Ter
|
|
ENST00000464550.5:n.463G>T
|
|
|
ENST00000471657.1:n.430G>T
|
|
|
ENST00000481757.5:n.2561G>T
|
|
|
ENST00000486058.5:n.1740G>T
|
|
|
ENST00000493398.5:n.773G>T
|
|
|
NM_018226.4:c.1627G>T
|
NP_060696.4:p.Glu543Ter
|
|
XM_005247036.3:c.1594G>T
|
XP_005247093.1:p.Glu532Ter
|
|
NM_018226.5:c.1627G>T
|
NP_060696.4:p.Glu543Ter
|
|
XM_005247036.4:c.1594G>T
|
XP_005247093.1:p.Glu532Ter
|
|
NM_018226.6:c.1627G>T
MANE Select
|
NP_060696.4:p.Glu543Ter
|
|